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This study examines chemokine modulation therapy combined with standard chemotherapy given before surgery in early-stage triple negative breast cancer. The medications used include Celecoxib, Cyclophosphamide, Doxorubicin, Paclitaxel, recombinant interferon alfa-2b, and Rintatolimod. Patients with resectable triple negative breast cancer who had no prior chemotherapy for this cancer could take part. It was conducted in Phase 1 and has been completed.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion Criteria: * Have pathologically confirmed diagnosis of resectable triple negative breast cancer (ASCO/CAP guidelines will be used to define triple negative breast cancer) * Must have measurable disease. Multi-centric disease is allowed. If patient has another lesion which is biopsied with ER/PR positive it will be Physician discretion for this eligibility criteria. * Prior therapy: No prior cytotoxic regimens are allowed for this malignancy. Participants may not have had prior chemotherapy, other targeted anticancer therapies, or prior radiation therapy to the ipsilateral breast for this malignancy. Prior bis-phosphonate therapy is allowed * Patient eligible for surgery as determined by patient's surgeon * Patient must have a lesion that amendable to biopsy, unless inaccessible and with PI approval * Have an Eastern Cooperative Oncology Group (ECOG) performance status of =\< 2 * Participants of child-bearing potential must agree to use adequate contraceptive methods (e.g., hormonal or barrier method of birth control; abstinence) prior to study entry. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately * Ability to swallow and retain oral medication * Ability to undergo magnetic resonance imaging (MRI) * Platelets \>= 100,000/uL * Hemoglobin \>= 9 g/dL * Absolute neutrophil count (ANC) \>= 1500/uL * Total bilirubin =\< institutional upper limit of normal (ULN) * Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase \[SGOT\]) and ALT (serum glutamate pyruvate transaminase \[SGPT\]) =\< 1.5 X institutional upper limit of normal (ULN) * Creatinine \< ULN OR creatinine clearance \>= 50 mL/min per Cockcroft-Gault equation for patients with creatinine levels greater than ULN * Left ventricular ejection fraction (LVEF) \>= 55%; if LVEF is \< 55% and patient is otherwise study-eligible, the principal investigator (PI) will discuss with cardiologist if patient is eligible to receive doxorubicin and participate in study * Participant or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee/Institutional Review Board approved written informed consent form prior to receiving any study related procedure * Participants on this study will be counseled on and are willing to use adequate contraceptive methods Exclusion Criteria: * Patients currently treated with systemic immunosuppressive agents, including steroids, are ineligible until 3 weeks after removal from immunosuppressive treatment * Patients with active autoimmune disease, requiring ongoing immunosuppressive therapy or history of transplantation * Diagnosis of invasive carcinoma within the last 3 years * Inflammatory breast cancer will be excluded from the study * Participants who have metallic surgical implants that are not compatible with an MRI machine are not eligible * Pregnant or nursing female participants * Unwilling or unable to follow protocol requirements * Patients with known serious mood disorders. (Major depression is an exclusion. Other stable mood disorders on stable therapy for \> 6 months may be allowed after consultation with PI) * Cardiac risk factors including: * Patients experiencing cardiac event(s) (acute coronary syndrome, myocardial infarction, or ischemia) within 3 months of signing consent * Patients with a New York Heart Association classification of III or IV * History of upper gastrointestinal ulceration, upper gastrointestinal bleeding, or upper gastrointestinal perforation within the past 3 years * Prior allergic reaction or hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs) or any drugs administered on protocol * Any history of allergy to sulfonamides * Any history of autoimmune hepatitis * Grade 1 or higher neuropathy * Any condition which in the investigator's opinion deems the participant an unsuitable candidate to receive study drug